Clearance Summary
PERCUPASS TUNNELING TOOL MODEL 3452 received FDA 510(k) clearance under submission number K772013, sponsored by Medtronic Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1977-10-28.
- Submission: K772013
- Applicant / Sponsor: Medtronic Vascular
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class I
- Regulation citation: 21 CFR 882.4535
- Decision date: 1977-10-28
Classification & Regulation
This clearance is catalogued under FDA product code HAO and 21 CFR 882.4535, within the Neurology review panel as a Class I device.